CO4950556A1 - QUINOLINE DERIVATIVES THAT HAVE A GROUP IMIDAZOLE AND COMPOSITIONS THAT CONTAIN THEM. - Google Patents

QUINOLINE DERIVATIVES THAT HAVE A GROUP IMIDAZOLE AND COMPOSITIONS THAT CONTAIN THEM.

Info

Publication number
CO4950556A1
CO4950556A1 CO98037149A CO98037149A CO4950556A1 CO 4950556 A1 CO4950556 A1 CO 4950556A1 CO 98037149 A CO98037149 A CO 98037149A CO 98037149 A CO98037149 A CO 98037149A CO 4950556 A1 CO4950556 A1 CO 4950556A1
Authority
CO
Colombia
Prior art keywords
group
compositions
contain
ncn
quinoline derivatives
Prior art date
Application number
CO98037149A
Other languages
Spanish (es)
Inventor
Rajeev S Bhide
Charles Z Ding
John T Hunt
Kim Soong-Hoom
Leftheris Katerina
Original Assignee
Bristol Myers Squibb Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of CO4950556A1 publication Critical patent/CO4950556A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings

Abstract

Un compuesto de la fórmula I o IIcaracterizado porque:1, m, r, s y t son 0 ó 1;n es 0, 1 ó 2;y se selecciona del grupo que consiste de CHR12 , SO2 , SO3 , CO , CO2 , O, NR13 , SO2 NR14 , CONR15 , C(NCN), C(NCN)NR16 , NR17 CO, NR18 SO2 , CONR19 NR20 , SO2 NR21 NR22 , S(O)(NR23 ), S(NR24 ) (NR25 ), o sin Y;Z se selecciona del grupo que consiste de CR12 , S, SO, SO2 , SO3 , CO, CO2 , O, NR13 , SO2 NR14 , CONR15 , NR26 NR27 , ONR28 , NR29 O, NR30 SO2 NR31 , NR32 SO2 , NR33 C(NCN), NR34 C(NCN)NR35 , NR36 CO, NR37 CONR38 , NR39 CO2 , OCONR40 , S(O)(NR41 ), S(NR42 ) NR43 ) o CHR12 ; o sin Z;R7 , R8 se seleccionan del grupo que consiste de hidrógeno halo, nitro, ciano y U-R44 ;U se selecciona del grupo que consiste de S, O, NR45 , CO, SO, SO2 , CO2 , NR46 CO2 , NR47 CONR48 , NR49 SO2 , NR50 SO2 NR51 , SO2 NR52 , NR53 CO, CONR54 , PO2 R55 y PO3 R56 o sin U;R9 , R10 , R12 , R13 , R14 , R15 , R16 , R17 , R18 , R19 , R20 , R21 , R22 , R23 , R24 , R25 ,R26 , R27 , R28 , R29 , R30 , R31 , R32 , R33 , R34 , R35 , R36 , R37 , R38 , R39 , R40 , R41 , R42 , R43 , R44 , R45 , R46 , R47 , R48 , R49 , R50 , R51 , R52 , R53 , R54 , R55 , R56 , R57 , R58 , R59 , se seleccionan del grupo que consiste de hidrógeno, alquilo inferior, arilo, heterociclo, alquilo sustituido o arilo;R11 y R44 se seleccionan del grupo que consiste de hidrógeno, alquilo, alquilo sustituido, alquenilo, alquenilo sustituido, alquinilo, alquinilo sustituido, aralquilo, cicloalquilo, arilo,...A compound of formula I or II characterized in that: 1, m, r, s and t are 0 or 1; n is 0, 1 or 2; and is selected from the group consisting of CHR12, SO2, SO3, CO, CO2, O, NR13, SO2 NR14, CONR15, C (NCN), C (NCN) NR16, NR17 CO, NR18 SO2, CONR19 NR20, SO2 NR21 NR22, S (O) (NR23), S (NR24) (NR25), or without Y ; Z is selected from the group consisting of CR12, S, SO, SO2, SO3, CO, CO2, O, NR13, SO2 NR14, CONR15, NR26 NR27, ONR28, NR29 O, NR30 SO2 NR31, NR32 SO2, NR33 C ( NCN), NR34 C (NCN) NR35, NR36 CO, NR37 CONR38, NR39 CO2, OCONR40, S (O) (NR41), S (NR42) NR43) or CHR12; or without Z; R7, R8 are selected from the group consisting of halo, nitro, cyano and U-R44 hydrogen; U is selected from the group consisting of S, O, NR45, CO, SO, SO2, CO2, NR46 CO2, NR47 CONR48, NR49 SO2, NR50 SO2 NR51, SO2 NR52, NR53 CO, CONR54, PO2 R55 and PO3 R56 or without U; R9, R10, R12, R13, R14, R15, R16, R17, R18, R19, R20, R21 , R22, R23, R24, R25, R26, R27, R28, R29, R30, R31, R32, R33, R34, R35, R36, R37, R38, R39, R40, R41, R42, R43, R44, R45, R46 , R47, R48, R49, R50, R51, R52, R53, R54, R55, R56, R57, R58, R59, are selected from the group consisting of hydrogen, lower alkyl, aryl, heterocycle, substituted alkyl or aryl; R11 and R44 are selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aralkyl, cycloalkyl, aryl, ...

CO98037149A 1997-07-02 1998-07-01 QUINOLINE DERIVATIVES THAT HAVE A GROUP IMIDAZOLE AND COMPOSITIONS THAT CONTAIN THEM. CO4950556A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US5159497P 1997-07-02 1997-07-02

Publications (1)

Publication Number Publication Date
CO4950556A1 true CO4950556A1 (en) 2000-09-01

Family

ID=21972255

Family Applications (1)

Application Number Title Priority Date Filing Date
CO98037149A CO4950556A1 (en) 1997-07-02 1998-07-01 QUINOLINE DERIVATIVES THAT HAVE A GROUP IMIDAZOLE AND COMPOSITIONS THAT CONTAIN THEM.

Country Status (24)

Country Link
US (2) US6387926B1 (en)
EP (1) EP0994856A4 (en)
JP (1) JP2002507989A (en)
KR (1) KR100385941B1 (en)
CN (1) CN1261880A (en)
AR (1) AR016304A1 (en)
AU (1) AU734721B2 (en)
BR (1) BR9810465A (en)
CA (1) CA2294530A1 (en)
CO (1) CO4950556A1 (en)
HU (1) HUP0004148A3 (en)
ID (1) ID24076A (en)
IL (1) IL133470A0 (en)
MY (1) MY117961A (en)
NO (1) NO316117B1 (en)
NZ (1) NZ501293A (en)
PE (1) PE86599A1 (en)
PL (1) PL337697A1 (en)
RU (1) RU2211838C2 (en)
TR (1) TR199903331T2 (en)
TW (1) TW527355B (en)
UY (1) UY25074A1 (en)
WO (1) WO1999001434A1 (en)
ZA (1) ZA985778B (en)

Families Citing this family (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6747023B1 (en) * 1998-08-11 2004-06-08 Daiichi Pharmaceutical Co., Ltd. Sulfonyl derivatives
AU754204B2 (en) * 1998-09-01 2002-11-07 Bristol-Myers Squibb Company Potassium channel inhibitors and method
AU2477400A (en) 1998-12-08 2000-06-26 Merck & Co., Inc. Inhibitors of prenyl-protein transferase
US6316436B1 (en) 1998-12-08 2001-11-13 Merck & Co., Inc. Inhibitors of prenyl-protein transferase
CA2395772C (en) * 1999-12-28 2010-09-28 Eisai Co., Ltd. Sulfonamide-containing heterocyclic compounds
GB0023915D0 (en) * 2000-09-29 2000-11-15 Inst Of Ophthalmology Treatment of neuroinflammatory disease
WO2002043733A1 (en) * 2000-11-28 2002-06-06 Janssen Pharmaceutica N.V. Farnesyl protein transferase inhibitors for the treatment of inflammatory bowel disease
FR2819510B1 (en) * 2001-01-18 2003-10-31 Servier Lab NOVEL CYCLO [C] AZEPANE COMPOUNDS, PROCESS FOR THEIR PREPARATION AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME
FR2819512B1 (en) * 2001-01-18 2003-02-21 Servier Lab NOVEL CYCLO [D] AZEPANE COMPOUNDS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
FR2825705B1 (en) 2001-06-08 2005-05-20 Aventis Pharma Sa NOVEL HETEROCYCLIC COMPOUNDS, THEIR PREPARATION AND THEIR USE AS MEDICAMENTS, IN PARTICULAR AS ANTI-BACTERIANS
US6740757B2 (en) * 2001-08-29 2004-05-25 Pfizer Inc Enantiomers of 6-[(4-chloro-phenyl)-hydroxy-(3-methyl-3h-imidazol-4-yl)-methyl]-4-[3-(3-hydroxy-3-methyl-but-1-ynyl)-phenyl]-1-methyl-1h-quinolin-2-one and salts thereof, useful in the treatment of cancer
FR2835186B1 (en) 2002-01-28 2006-10-20 Aventis Pharma Sa NOVEL HETEROCYCLIC COMPOUNDS ACTIVE AS BETA-LACTAMASES INHIBITORS
AU2003259717A1 (en) * 2002-08-07 2004-02-25 Bristol-Myers Squibb Company Modulators of rabggt and methods of use thereof
FR2844273B1 (en) 2002-09-05 2008-04-04 Aventis Pharma Sa NOVEL HETEROCYCLIC COMPOUNDS, METHOD AND INTERMEDIARY PREPARATION AND USE AS MEDICAMENT, IN PARTICULAR AS INHIBITORS OF BETA-LACTAMASES AND ANTI-BACTERIALS.
ATE443048T1 (en) * 2002-11-20 2009-10-15 Japan Tobacco Inc 4-OXOCINOLINE COMPOUNDS AND THEIR USE AS HIV INTEGRASE INHIBITORS
WO2005007628A1 (en) 2003-07-11 2005-01-27 Bristol-Myers Squibb Company Tetrahydroquinoline derivatives as cannabinoid receptor modulators
JP4691041B2 (en) 2003-11-20 2011-06-01 チルドレンズ ホスピタル メディカル センター GTPase inhibitors and methods of use
US20050272722A1 (en) * 2004-03-18 2005-12-08 The Brigham And Women's Hospital, Inc. Methods for the treatment of synucleinopathies
WO2005089502A2 (en) * 2004-03-18 2005-09-29 The Brigham And Women's Hospital, Inc. Methods for the treatment of synucleinopathies
JP2007538004A (en) * 2004-03-18 2007-12-27 ザ ブライハム アンド ウイメンズ ホスピタル, インコーポレイテッド How to treat synucleinopathy
US20070293539A1 (en) * 2004-03-18 2007-12-20 Lansbury Peter T Methods for the treatment of synucleinopathies
US20050288298A1 (en) * 2004-03-18 2005-12-29 The Brigham And Women's Hospital, Inc. Methods for the treatment of synucleinopathies
WO2005089518A2 (en) * 2004-03-18 2005-09-29 The Brigham And Women's Hospital, Inc. Uch-l1 expression and cancer therapy
US7531554B2 (en) * 2004-05-20 2009-05-12 Japan Tobacco Inc. 4-oxoquinoline compound and use thereof as HIV integrase inhibitor
US20060160850A1 (en) * 2005-01-18 2006-07-20 Chongqing Sun Bicyclic heterocycles as cannabinoid receptor modulators
US20060194821A1 (en) * 2005-02-18 2006-08-31 The Brigham And Women's Hospital, Inc. Compounds inhibiting the aggregation of superoxide dismutase-1
WO2006101937A1 (en) 2005-03-18 2006-09-28 Janssen Pharmaceutica N.V. Acylhydrazones as kinase modulators
EP1904069B1 (en) 2005-07-15 2018-06-13 Albany Molecular Research, Inc. Aryl-and heteroaryl-substituted tetrahydrobenzazepines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin
EP1920048A4 (en) 2005-07-29 2009-12-09 Childrens Hosp Medical Center Gtpase inhibitors and methods of use and crystal structure of rac-1 gtpase
US8003624B2 (en) * 2005-08-25 2011-08-23 Schering Corporation Functionally selective ALPHA2C adrenoreceptor agonists
EP2545919A1 (en) * 2005-12-23 2013-01-16 Link Medicine Corporation Treatment of synucleinopathies
US8383819B2 (en) * 2006-03-06 2013-02-26 Japan Tobacco Inc. Method for producing 4-oxoquinoline compound
CA2650520A1 (en) * 2006-04-24 2008-01-31 Gloucester Pharmaceuticals Treatment of ras-expressing tumors
AU2007321376A1 (en) * 2006-11-16 2008-05-22 F. Hoffmann-La Roche Ag Substituted 4-imidazoles
CN101686982A (en) * 2007-05-10 2010-03-31 Amr科技公司 The purposes of the tetrahydro benzo azepine that aryloxy group and heteroaryloxy replace and blocking-up norepinephrine, dopamine and 5-hydroxy tryptamine reuptake
FR2920773B1 (en) * 2007-09-11 2009-10-23 Servier Lab 1,2,4,5-TETRAHYDRO-3H-BENZAZEPINES DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
WO2009079765A1 (en) * 2007-12-21 2009-07-02 Cascade Therapeutics Inc. Compounds with activity at the 5-ht2c receptor
WO2009151683A2 (en) * 2008-03-12 2009-12-17 Link Medicine Corporation Quinolinone farnesyl transferase inhibitors for the treatment of synucleinopathies and other indications
US20100331363A1 (en) * 2008-11-13 2010-12-30 Link Medicine Corporation Treatment of mitochondrial disorders using a farnesyl transferase inhibitor
US20110060005A1 (en) * 2008-11-13 2011-03-10 Link Medicine Corporation Treatment of mitochondrial disorders using a farnesyl transferase inhibitor
WO2010057006A1 (en) * 2008-11-13 2010-05-20 Link Medicine Corporation Azaquinolinone derivatives and uses thereof
WO2013064231A1 (en) 2011-10-31 2013-05-10 Phenex Pharmaceuticals Ag SEVEN-MEMBERED SULFONAMIDES AS MODULATORS OF RAR-RELATED ORPHAN RECEPTOR-GAMMA (RORγ, NR1F3)
WO2013166043A1 (en) 2012-05-02 2013-11-07 Children's Hospital Medical Center Rejuvenation of precursor cells
CN103864765B (en) * 2014-03-05 2016-02-10 天津药物研究院 Benzazepine analog derivative containing five-membered ring, Preparation Method And The Use
US10028503B2 (en) 2014-06-18 2018-07-24 Children's Hospital Medical Center Platelet storage methods and compositions for same
ES2926579T3 (en) 2016-05-05 2022-10-27 Laurus Labs Ltd Process for the preparation of intermediate compounds useful in the preparation of inhibitors of the Hepatitis C virus (HCV)
WO2017213210A1 (en) * 2016-06-10 2017-12-14 武田薬品工業株式会社 Heterocyclic compound

Family Cites Families (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4110536A (en) 1977-04-18 1978-08-29 Miles Laboratories, Inc. Derivatives of 5-(indol-3-yl)hydantoin
JPS5852256A (en) * 1981-09-24 1983-03-28 Nippon Nohyaku Co Ltd Substituted or unsubstituted fatty acid amide derivative and its salt
JPS60222479A (en) * 1984-04-20 1985-11-07 Nippon Tokushu Noyaku Seizo Kk Tetrahydroquinolin-1-ylcarbonylimidazole derivative, its intermediate, their production and herbicide and fungicide therefrom
US4576957A (en) 1984-07-05 1986-03-18 American Cyanamid Company N-(Substituted phenyl)-N'-[(1H-imidazol-1-yl) and (1H-1,2,4-triazol-1-yl)alkyl]ureas
JPS6160682A (en) * 1984-08-30 1986-03-28 Nippon Tokushu Noyaku Seizo Kk Tetrahydroquinolin-1-ylcarbonylimidazole derivative, its intermediate, its production, herbicide, agricultural and horticultural fungicide
JPS6168487A (en) * 1984-09-12 1986-04-08 Sumitomo Chem Co Ltd Carbamoylazole derivative, its production, and herbicide comprising it as active ingredient
US5017584A (en) 1984-12-20 1991-05-21 Sterling Drug Inc. Antidepressant 2-(4,5-dihydro-1H-imidazolyl)-dihydro-1H-indoles, -1,2,3,4-tetrahydroquinolines and -1H-indoles, and methods of use thereas
JPS61227506A (en) * 1985-04-01 1986-10-09 Nippon Tokushu Noyaku Seizo Kk Carbamoylimidazole, intermediate and, production thereof and herbicide, agricultural and horticultural fungicide
JPS61280408A (en) * 1985-06-03 1986-12-11 Sumitomo Chem Co Ltd Tobacco sucker inhibitor
JPS63270678A (en) * 1987-04-30 1988-11-08 Mitsui Petrochem Ind Ltd Novel nitrogen-containing compound
JP2652249B2 (en) 1989-08-22 1997-09-10 進 根本 Key knob cover
US5374615A (en) 1990-10-31 1994-12-20 E. R. Squibb & Sons, Inc. Indole- and benzimidazole-substituted imidazole and benzimidazole derivatives
EP0485890A3 (en) * 1990-11-16 1992-07-08 Hoechst Aktiengesellschaft Use of 2,3-disubstituate 1-azolyl-propane for inhibiting the pathogenic growth phase of dimorph yeast cell
US5633376A (en) 1990-12-28 1997-05-27 Neurogen Corporation Certain aminomethyl phenylimidazole derivatives; and 4-aryl substituted piperazinyl and piperidinylmethyl phenylimidazole derivatives; a new class of dopamine receptor subtype ligands
US5371227A (en) 1991-10-28 1994-12-06 Synthelabo Quinoline derivatives, process for their preparation, and their therapeutic applications
US5322950A (en) 1991-12-05 1994-06-21 Warner-Lambert Company Imidazole with angiotensin II antagonist properties
US5656644A (en) 1994-07-20 1997-08-12 Smithkline Beecham Corporation Pyridyl imidazoles
GB9206757D0 (en) 1992-03-27 1992-05-13 Ferring Bv Novel peptide receptor ligands
US5726197A (en) 1992-11-02 1998-03-10 Syntex (U.S.A.) Inc. Isoindolinyl derivatives
US5284841A (en) 1993-02-04 1994-02-08 Merck & Co., Inc. Benzo-fused lactams promote release of growth hormone
CA2118985A1 (en) 1993-04-02 1994-10-03 Dinesh V. Patel Heterocyclic inhibitors of farnesyl protein transferase
US5523317A (en) 1993-07-05 1996-06-04 Nippon Chemiphar Co., Ltd. Method of reducing blood pressure
US5576437A (en) 1993-12-17 1996-11-19 The Procter & Gamble Company 7-(2-imidazolnylamino) quinoline compounds useful as alpha-2 adrenoceptor agonists
ES2146307T3 (en) 1993-12-17 2000-08-01 Procter & Gamble COMPOUNDS OF 6- (2-IMIDAZOLINYLAMINE) QUINOLINE USEFUL AS 2-ALPHA ADRENOCEPTOR AGONISTS.
HUT72440A (en) * 1994-03-31 1996-04-29 Bristol Myers Squibb Co Imidazole-containing inhibitors of farnesyl protein transferase and pharmaceutical compositions containing them
US5607939A (en) 1994-04-28 1997-03-04 Takeda Chemical Industries, Ltd. Condensed heterocyclic compounds, their production and use
US5616601A (en) 1994-07-28 1997-04-01 Gd Searle & Co 1,2-aryl and heteroaryl substituted imidazolyl compounds for the treatment of inflammation
US5880141A (en) * 1995-06-07 1999-03-09 Sugen, Inc. Benzylidene-Z-indoline compounds for the treatment of disease
TW436484B (en) 1996-04-24 2001-05-28 Dev Center Biotechnology 1,2,3,4-tetrahydroisoquinoline derivatives having a nitrogen-containing heterocyclic methyl substituent, the preparation process and pharmaceutical composition thereof
WO1998002432A1 (en) 1996-07-16 1998-01-22 Takeda Chemical Industries, Ltd. Bicyclic compounds for controlling micturition
UA60311C2 (en) 1996-10-02 2003-10-15 Смітклайн Бічам Корпорейшн Vitronectin receptor antagonists

Also Published As

Publication number Publication date
TW527355B (en) 2003-04-11
TR199903331T2 (en) 2000-06-21
NO316117B1 (en) 2003-12-15
ZA985778B (en) 2000-01-20
ID24076A (en) 2000-07-06
MY117961A (en) 2004-08-30
NO996571D0 (en) 1999-12-30
AR016304A1 (en) 2001-07-04
NO996571L (en) 2000-02-23
BR9810465A (en) 2002-04-16
IL133470A0 (en) 2001-04-30
KR20010014258A (en) 2001-02-26
JP2002507989A (en) 2002-03-12
EP0994856A4 (en) 2000-12-06
HUP0004148A2 (en) 2001-10-28
HUP0004148A3 (en) 2002-09-30
PL337697A1 (en) 2000-08-28
EP0994856A1 (en) 2000-04-26
US6602883B1 (en) 2003-08-05
AU7971998A (en) 1999-01-25
CN1261880A (en) 2000-08-02
UY25074A1 (en) 2000-12-29
CA2294530A1 (en) 1999-01-14
NZ501293A (en) 2001-10-26
PE86599A1 (en) 1999-11-28
WO1999001434A1 (en) 1999-01-14
AU734721B2 (en) 2001-06-21
KR100385941B1 (en) 2003-06-09
US6387926B1 (en) 2002-05-14
RU2211838C2 (en) 2003-09-10

Similar Documents

Publication Publication Date Title
CO4950556A1 (en) QUINOLINE DERIVATIVES THAT HAVE A GROUP IMIDAZOLE AND COMPOSITIONS THAT CONTAIN THEM.
AR015774A1 (en) EPOTILONE DERIVATIVES 12,13-MODIFIED AND ITS SALTS
AR045761A1 (en) DERIVATIVES OF 2-PIRIDONA AS INHIBITORS OF ELASTASA DE NEUTROFILOS
AR030432A1 (en) USE OF QUINAZOLINE DERIVATIVES IN THE PREPARATION OF A MEDICINAL PRODUCT TO BE USED IN THE INHIBITION OF AURORA QUINASA2, RELATED COMPOUNDS, AND PHARMACEUTICAL COMPOSITION.
TR199903270T2 (en) Omeprazole sodium salt.
AR045691A1 (en) HETEROARILAMIDE DERIVATIVES AS P2X7 ANTAGONIST RECEIVERS AND THEIR USES
AR037881A1 (en) USE OF OXINDOL DERIVATIVES
BG62615B1 (en) (imidazol-5-yl)methyl-2-quinoline derivatives inhibiting pharnesyl protein transferase
NO910863L (en) N- (4-PIPERIDINYL) (DIHYDROBENZOFURAN OR DIHYDRO-2H-BENZOPYRANE) CARBOXAMIDE DERIVATIVES AND PROCEDURES FOR THEIR PREPARATION.
HK1028032A1 (en) Pyridonecarboxylic acid derivatives or their salts, and antibacterial agent comprising the same as the active ingredient
NZ334125A (en) Quinoline derivatives inhibiting the effect of growth factors such as VEGF
TR199900827T2 (en) Use of cyclooxygenase-2 inhibitors in the treatment and prevention of neoplasia.
AR050598A2 (en) SYNERGIC FUNGUICIDE COMPOSITION, PROCEDURE TO COMBAT HARMFUL FUNGES AND USE OF COMPOUNDS THAT INTEGRATE SUCH COMPOSITION FOR THE PREPARATION OF SUCH SYNERGIC MIXTURES
AR060042A1 (en) NANOPARTICLES UNDERSTANDING A PDGF RECEPTOR THYROSINE KINASE INHIBITOR
PL350123A1 (en) Tetrahydropyran derivatives and their use as therapeutic agents
TR200000414T2 (en) 2- (4-Aryl or heteroaryl-piperazin-1-ylmethyl) -1H-indole derivatives.
AR042733A1 (en) PIRIDINE DERIVATIVES USED AS INHIBITORS OF THE NA + / CA2 + EXCHANGE MECHANISM
NZ502180A (en) 6-Azauracil derivatives and their use as IL-5 inhibitors
DE69621651D1 (en) AZAHEXAN DERIVATIVES AS SUBSTRATISOSTERES OF RETROVIRAL ASPARTATE PROTEASES
ATE248819T1 (en) CYANOGUANIDINES AS CELL PROLIFERATION INHIBITORS
MY127758A (en) Derivatives of homopiperidinyl substituted benzimidazole analogues
CO5221028A1 (en) FUNGICIDE MIXTING THAT INCLUDES DERIVATIVES OF ETER QUINOLINE AND CARBAMATES
DE60000234D1 (en) Indole compounds, their use in dyeing and making up keratin fibers, compositions containing them and dyeing processes
NO164836C (en) ANALOGY PROCEDURE FOR THE PREPARATION OF NEW THERAPEUTICALLY ACTIVE NAFTYRIDINE DERIVATIVES.
DE50001988D1 (en) DOLLAR g (a) - DOLLAR g (a) 'SUBSTITUTED N-ALKYL-3-ALKENYLBENZOYL-PYRAZOLE DERIVATIVES